A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657830



Internal ID21606135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20325775..20325775hg38UCSC Ensembl
chr14:20793934..20793934hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085345
SamplesNA19239
Known GenesCCNB1IP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657830
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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